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PRODIGY iConnect Blood Glucose Monitoring System

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K142785
510(k) Type
Traditional
Applicant
Ok Biotech Co., Ltd.
Country
Taiwan
FDA Decision
Substantially Equivalent
Decision Date
12/17/2015
Days to Decision
447 days
Submission Type
Summary

PRODIGY iConnect Blood Glucose Monitoring System

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K142785
510(k) Type
Traditional
Applicant
Ok Biotech Co., Ltd.
Country
Taiwan
FDA Decision
Substantially Equivalent
Decision Date
12/17/2015
Days to Decision
447 days
Submission Type
Summary